Inhibition of tumor cell kinetics and serum insulin growth factor I levels by octreotide in colorectal cancer patients von Cascinu, S, Del Ferro, E, Grianti, C, Ligi, M, Ghiselli, R, Foglietti, G, Saba, V, Lungarotti, F, Catalano, G

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Cytokinetic effects of interferon in colorectal cancer tumors : implications in the design of the interferon/5-fluorouracil combinations von CASCINU, S, DEL FERRO, E, CATALANO, G, FEDELI, A, GRIANTI, C, FOGLIETTI, G, OLIVIERI, Q, ACETOSO, M, BARTOLUCCI, M, SABA, V, LUNGAROTTI, F

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Adjuvant Chemotherapy in Completely Resected Gastric Cancer: A Randomized Phase III Trial Conducted by GOIRC von Di Costanzo, Francesco, Gasperoni, Silvia, Manzione, Luigi, Bisagni, Giancarlo, Labianca, Roberto, Bravi, Stefano, Cortesi, Enrico, Carlini, Paolo, Bracci, Raffaella, Tomao, Silverio, Messerini, Luca, Arcangeli, Annarosa, Torri, Valter, Bilancia, Domenico, Floriani, Irene, Tonato, Maurizio

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The combined maternal administration of magnesium sulfate and aminophylline reduces intraventricular hemorrhage in very preterm neonates von Di Renzo, Gian Carlo, Mignosa, Marcella, Gerli, Sandro, Burnelli, Liliana, Luzi, Giuseppe, Clerici, Graziano, Taddei, Fabiana, Marinelli, Doretta, Bragetti, Patrizia, Mezzetti, Daniele, Torre, Benedetta Della, Fantauzzi, Alessandra, Lungarotti, Maria Serena

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Reply von Di Renzo, G.C., Mignosa, M.M., Gerli, S., Burnelli, L., Luzi, G., Clerici, G., Taddei, F., Marinelli, D., Bragetti, B., Mezzetti, D., Della Torre, B., Fantauzzi, A., Lungarotti, M.S.

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The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region von WIJKER, M, LIGTENBERG, M. J. L, LUNGAROTTI, M. S, ARWERT, F, SCHOUTE, F, DEFESCHE, J. C, PALS, G, BOLHUIS, P. A, ROPERS, H. H, HULSEBOS, T. J. M, MENKO, F. H, VAN OOST, B. A

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Post-discharge nutrition of the very low-birthweight infant: interim results of the multicentric GAMMA study von Agosti, M, Vegni, C, Calciolari, G, Marini, A

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Audiological findings in down's children von Maurizi, M., Ottaviani, F., Paludetti, G., Lungarotti, S.

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Hypomelanosis of ito associated with chromosomal translocation involving Xp11 von Lungarotti, M. Serena, Martello, Cecilia, Calabro, Anna, Baldari, Franco, Mariotti, Giacomo

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Craniosynostosis and unilateral ulnar aplasia von Calabro, Anna, Lungarotti, M. Serena, Latini, S., Molinari, Daniela, Opitz, John M., Reynolds, James F.

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Incidence of Congenital Rubella Syndrome in 19 Regions of Europe in 1980-1986 von De La Mata, I., De Wals, P., Dolk, H., Lechat, M. F., Beckers, R., Borlee, I., Lys, F., Zori, R., Goujard, J., Stoll, C., Ayme, S., Hansen-Koenig, D., Karkut, G., Galanti, C., Marchi, M., Bianchi, F., Calabro, A., Lungarotti, S., Calzolari, E., Radic, A., Lillis, F., Stone, D., Harris, F., Nevin, N., Kate, L. Ten, Svel, I., Ligutic, I., Cuschieri, A.

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Omphalocele and gastroschisis: A collaborative study of five Italian congenital malformation registries von Calzolari, E., Volpato, S., Bianchi, F., Cianciulli, D., Tenconi, R., Clementi, M., Calabro, A., Lungarotti, S., Mastroiacovo, P. P., Botto, L., Spagnolo, A., Milan, M.

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Multiple congenital anomalies associated with apparently normal maternal intake of vitamin A: A phenocopy of the isotretinoin syndrome? von Lungarotti, M. S., Marinelli, D., Mariani, T., Calabro, A., Opitz, John M., Reynolds, James F.

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Familial situs inversus and congenital heart defects von Calabro, Al, Taraschi, A., Lungarotti, M. S., Ferdinandi, A., Opitz, John M., Reynolds, James F.

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De novo duplication 1q32-q42: variability of phenotypic features in partial lq trisomics von Lungarotti, M S, Falorni, A, Calabro, A, Passalacqua, F, Dallapiccola, B

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Characterization of serum alkaline phosphatase in infancy and childhood von Cao, A., Coppa, G., Trabalza, N., Marcucci, F., Virgiliis, S., Lungarotti, S., Furbetta, M.

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